Canonical Allele Identifier: CA2785233491
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851720G>T , CM000671.2:g.97851720G>T GRCh38
NC_000009.11:g.100614002G>T , CM000671.1:g.100614002G>T GRCh37
NC_000009.10:g.99653823G>T NCBI36
NG_011979.1:g.3466G>T

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1156C>A
XR_930159.1:n.218+1156C>A
XR_930160.1:n.218+1156C>A
XR_930161.1:n.218+1156C>A
NR_147055.1:n.165+1196C>A